NDC 0093-5046-01
Dexmethylphenidate Hydrochloride 35 mg/1
Dexmethylphenidate Hydrochloride · CAPSULE, EXTENDED RELEASE
Dexmethylphenidate Hydrochloride is a capsule, extended release containing dexmethylphenidate hydrochloride at a strength of 35 mg/1. Manufactured by Teva Pharmaceuticals USA, Inc..
Key Facts
- Brand Name
- Dexmethylphenidate Hydrochloride
- Generic Name
- Dexmethylphenidate Hydrochloride
- NDC Code (Package)
0093-5046-01- NDC Code (Product)
0093-5046- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Strength
- 35 mg/1
- Dosage Form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA202731
- Marketing Start
- 07/05/2017
Recall History
No Recall HistoryView Full Drug Page
Dexmethylphenidate Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.